Chang C S, Hsieh P F, Chia L G, Chen C C, Chen C C, Pan S T, Wang Y C
Department of Medicine, Taichung Veterans General Hospital, Taiwan, R.O.C.
Zhonghua Yi Xue Za Zhi (Taipei). 1997 Dec;60(6):316-20.
A rare case of histology-proved giant congenital melanocytic nevus (GCMN) with symptomatic leptomeningeal melanocytosis is reported. A 26-year-old man had had a large patch of pigmented nevus over his back and left arm since birth. He had begun to have seizures as well as symptoms and signs of increased intracranial pressure about six months before admission. Serial computed tomography of brain showed hydrocephalus, diffuse leptomeningeal enhancement and multiple well-enhanced, rapid-growing nodules on the surface of the cerebellum and left parietal lobe. Magnetic resonance imaging (MRI) revealed T1 shortening of leptomeninges on precontrast T1 weighted imaging. Skin biopsy was done twice and showed intradermal nevus. Biopsy on one of the intracranial nodules revealed malignant melanoma arising in the melanocytosis. He died one year after the onset of neurologic symptoms. For early diagnosis of neurocutaneous melanocytosis, we suggest 1) MRI, and 2) leptomeningeal biopsy in patients with suspected leptomeningeal malignant melanoma.
报告了一例经组织学证实的巨大先天性黑素细胞痣(GCMN)合并症状性软脑膜黑素沉着症的罕见病例。一名26岁男性自出生以来背部和左臂有一大片色素痣。入院前约六个月,他开始出现癫痫发作以及颅内压升高的症状和体征。脑部系列计算机断层扫描显示脑积水、弥漫性软脑膜强化以及小脑和左顶叶表面多个强化良好、快速生长的结节。磁共振成像(MRI)在对比前T1加权成像上显示软脑膜T1缩短。皮肤活检进行了两次,显示为皮内痣。对其中一个颅内结节的活检显示黑素沉着症中出现恶性黑色素瘤。他在出现神经症状一年后死亡。对于神经皮肤黑素沉着症的早期诊断,我们建议:1)MRI;2)对疑似软脑膜恶性黑色素瘤的患者进行软脑膜活检。